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Goeldi's Monkey (Callimico goeldii)
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Order: Primates
Family: Callitrichidae - Callicominidae(nae)
1) General Zoological Data
The Goeldi's monkey is one of the many South American tree-dwelling small primates in Amazonia whose ecology and general characteristics have been described in detail by Heltne et al. (1981). It is considered to be an endangered species. Although similar in size to marmosets and tamarins, these species differ in many respects. Goeldi's monkey for instance does not produce twins and has a third molar tooth, absent in marmosets and tamarins. This is but one reason why it is generally considered to be more primitive. It is presumed that the Goeldi's monkey, one of the "dwarf species", split off the ancestral stock of South American primates prior to the development of marmosets (Dutrillaux et al., 1988). These authors discussed the presumed phylogeny in detail. Martin (1992), who considered this problem in modern detail, felt nevertheless that the species should be classed with other callithricids, rather than in a placed into a separate family. That publication summarizes all the controversial views that pertain to the placement of this species with marmosets and tamarins into one monophyletic group. Some controversy, however, still exists in the appropriate assignment of this animal. Longevity of about 18 years.
Goeldi's monkeys at San Diego Zoo.
2) General Gestational Data
Gestational length is approximately (150)-155 days with a singleton born. Twins occur only rarely in captivity. Newborns weigh between 30-50 g; adults are 393-860 g (Nowak, 1999).
3) Implantation
No studies of early implantation have been described for this species. The uterus is unicornuate.
4) General Characterization of the Placenta
Goeldi's monkey has a bidiscoid placenta with a villous, hemochorial implantation. The only report of its structure comes from Soma & Kada (1989) who observed two placentas. Both of these were from a stillborn animals and at least one pregnancy was deemed to have been premature, at 110 days gestation. One neonate weighed 56 g, the placenta weighed 4, and 5 g respectively and measured 2 x 2 x 0.6, 1.6 x 6 x0.4 cm, and 2 x 2 x 0.4, 3 x 2 x 0.5 cm. The two lobes were separated by 2.4 and 4 cm of membranes. Both had infarcts and the decidual necrosis at the floor was pronounced. They described the structure as "trabecular - pseudolabyrinthine". The histologic slides shown here come from a third placenta that was kindly donated to me from the Brookfield Zoo, Chicago. It also was from a stillborn term fetus, but macroscopic details were not supplied. The features are entirely those as of the previous authors' observations.
Placenta of Goeldi's monkey from publication of Soma and Kada (1989). The photograph was kindly supplied by Dr. Hiroaki Soma, Tokyo.
Macroscopic appearance of Goeldi placenta with fused disks, one smaller than the other.
5) Details of fetal/maternal barrier
Surface of placenta with detached amnion and the chorion above, villous tissue below.
Large chorioallantoic artery in chorion above, amnion at top left.
Villous structure of Goeldi's monkey. Note the absence of hematopoiesis in the villi.
The "floor" of a mature Goeldi's monkey placenta showing much decidual necrosis, and fibrin accumulation.
Higher magnification of villous structure with sparse syncytium and no villous hematopoiesis.
In contrast to tamarins, none of the three placentas observed by Soma and Kada (1989) and those seen by myself had villous hematopoiesis. There is an unusual amount of basal decidual necrosis, similar to what is seen in tamarins. The villous structure is somewhat trabecular, but not so pronounced as that of tamarins. The trophoblast is single-layered by light microscopy at least in term placentas. It is likely, however, that electron microscopy would disclose cytotrophoblast underlying the syncytium. At the implantation site, numerous large "X-cells" (extravillous trophoblast) are present. No such deposits of extravillous trophoblast exist in the villous portion of the placenta, unlike that seen in simians.
6) Umbilical cord
The umbilical cords of the two placentas described by Soma & Kada (1989) were 1.5 and 2.5 cm in length and had four blood vessels. They were marginally inserted on one disk and connected to the other disk by large membranous vessels. Spirals and ducts of any kind were not described.
7) Uteroplacental circulation
No studies have been published.
8) Extraplacental membranes
The amnion is thin and avascular with a single layer of epithelium. One placenta had a tiny, yellow yolk sac remnant beneath the amnion. There is a small amount of decidua capsularis.
9) Trophoblast external to barrier
This has not been observed, as no implanted placenta has been described. The decidual arterioles present in my specimen, however had no trophoblastic infiltration, although extravillous trophoblast is amply present in the decidua basalis.
10) Endometrium
The decidua basalis has much apparently normal necrosis and fibrin deposition. Nevertheless, the intervillous circulation was intact in all three placentas.
The "floor" of mature placentas always has a large amount of fibrin and fibrinoid accumulation, in addition to decidual necrosis. The blue cells are "X-cells" (extravillous trophoblast).
11) Various features
No other remarkable endometrial features have been recorded.
12) Endocrinology
Soma and Kada (1989) stained their placentas with anti-hCG antibodies and failed to demonstrate the presence of gonadotropins in that manner. Ziegler et al. (1990), on the other hand, identified urinary chorionic gonadotropins 18 days after presumed ovulation, with elevated titers remaining to day 45 days. The polyestrous animals have a cycle of 22-24 days, estrus lasting 7 days. Other endocrine studies come from Carroll et al. (1990) and Ziegler et al. (1990).
13) Genetics
Goeldi's monkeys have typically 48 chromosomes (Bender & Mettler, 1960; Chiarelli, 1980). Initially, a XX/XO sex determining mechanism was suspected (Hsu & Hampton, 1970). Subsequently the mystery was solved when a chromosomal error was described in a male animal. It had a fusion of the Y-chromosome to autosome # 23 (Dutrillaux et al., 1988). The animal appeared to be normal. The publication gives details of chromosomal banding patterns. A study of repetitive DNA provided additional support for the current phylogenetic position of this species (Montagnon, et al., 1993). Similar conclusions were also derived from the study of genes determining the v. Willebrand factor (Chaves, et al., 1999). No hybrids have been described.
14) Immunology
No studies are known to me.
15) Pathological features
Infarcts were present in two of the three placentas of stillborn fetuses. Callithrichids, including Goeldi's monkey, are extremely susceptible to infection with lymphocytic choriomeningitis virus (Asper et al., 2001). It is transmitted by wild mice and can be fatal with hepatitis. Pseudotuberculosis due to Yersinia pseudotuberculosis appears to be endemic at Jersey with death resulting in some animals (Bielli et al., 1999).
16) Physiologic data
I know of no data relevant to this section.
17) Other resources
Few cell lines are available from CRES through Dr. Oliver Ryder at: [email protected]
18) Other remarks - What additional Information is needed?
It would be helpful to have an implanted placenta described and one of live births. Moreover, the data on umbilical cord and endocrinology are woefully inadequate.
Acknowledgement
The animal photograph of this chapter comes from the Zoological Society of San Diego.
Get access to all handy features included in the IVIS website
- Get unlimited access to books, proceedings and journals.
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Asper, M., Hofmann, P., Osmann, C., Funk, J., Metzger, C., Bruns, M., Kaup, F.J., Schmitz, H. and Gunther, S.: First outbreak of callithrichid hepatitis in Germany: genetic characterization of the causative lymphocytic choriomeningitis virus strain. Virology 284:203-213, 2001.
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Affiliation of the authors at the time of publication
Department of Reproductive Medicine and Pathology, School of Medecine, University of California, San Diego, CA, USA.
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